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A7824

6-Aminocaproic acid

synthetic (organic), ≥99%, antifibrinolytic agent, powder

Synonym(s):

ε-Aminocaproic acid, 6-Aminohexanoic acid, EACA

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About This Item

Linear Formula:
H2N(CH2)5CO2H
CAS Number:
Molecular Weight:
131.17
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
200-469-3
MDL number:
Beilstein/REAXYS Number:
906872
Assay:
≥99%
Form:
powder
Grade:
biotech. grade
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Product Name

6-Aminocaproic acid, BioUltra, ≥99%

biological source

synthetic (organic)

Quality Segment

grade

biotech. grade

product line

BioUltra

assay

≥99%

form

powder

technique(s)

cell culture | mammalian: suitable

impurities

≤0.005% Phosphorus (P), ≤0.1% Insoluble matter

ign. residue

≤0.1%

mp

207-209 °C (dec.) (lit.)

solubility

H2O: 0.5 M, clear, colorless

anion traces

chloride (Cl-): ≤0.05%, sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%, Ca: ≤0.005%, Cu: ≤0.0005%, Fe: ≤0.0005%, K: ≤0.005%, Mg: ≤0.001%, NH4+: ≤0.05%, Na: ≤0.02%, Pb: ≤0.001%, Zn: ≤0.0005%

storage temp.

room temp

SMILES string

NCCCCCC(O)=O

InChI

1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)

InChI key

SLXKOJJOQWFEFD-UHFFFAOYSA-N

Gene Information

human ... PLAT(5327), PLG(5340)
rat ... Ppm1a(24666)

Biochem/physiol Actions

Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis.
Lysine analog. Promotes rapid dissociation of plasmin, thereby inhibiting the activation of plasminogen and subsequent fibrinolysis. Reported to inhibit plasminogen binding to activated platelets. An early report indicated that it inhibits the activation of the first component of the complement system. Binds and inactivates Carboxypeptidase B.

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This Item
A2504A04200008.00145
grade

biotech. grade

grade

-

grade

pharmaceutical primary standard

grade

synthesis grade

assay

≥99%

assay

≥99% (titration)

assay

-

assay

≥99% (HClO4)

Quality Level

300

Quality Level

300

Quality Level

-

Quality Level

200

form

powder

form

powder

form

-

form

crystals

storage temp.

room temp

storage temp.

-

storage temp.

2-8°C

storage temp.

2-30°C

solubility

H2O: 0.5 M, clear, colorless

solubility

H2O: 50 mg/mL

solubility

-

solubility

587.55 g/L


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Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

404.6 - 408.2 °F

flash_point_c

207 - 209 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Tijana Jovanovic-Talisman et al.
Methods in cell biology, 122, 379-393 (2014-05-27)
In vitro mimics of cellular machines have been recently engineered and utilized to investigate processes within cells. These devices can provide novel insights into biological mechanisms and have the potential to improve biotechnological processes such as separation. In particular, several
Robert A Gaultney et al.
PloS one, 8(9), e75643-e75643 (2013-10-03)
The causative agent of Lyme disease, Borrelia burgdorferi, codes for several known fibronectin-binding proteins. Fibronectin a common the target of diverse bacterial pathogens, and has been shown to be essential in allowing for the development of certain disease states. Another
Weining Bian et al.
Nature protocols, 4(10), 1522-1534 (2009-10-03)
This protocol describes a cell/hydrogel molding method for precise and reproducible biomimetic fabrication of three-dimensional (3D) muscle tissue architectures in vitro. Using a high aspect ratio soft lithography technique, we fabricate polydimethylsiloxane (PDMS) molds containing arrays of mesoscopic posts with



Global Trade Item Number

SKUGTIN
A7824-25G04061833386484
A7824-100G04061833386460
A7824-500G04061832938868
A7824-1KG04061833386477

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